Associate Clinical Project Management Director, IQB Immuno-Oncology and Cell and Gene Therapy (Spain)
IQVIA Barcelona
Experteer Overview
As Associate Clinical Project Management Director, you will lead and oversee studies to ensure timely, high-quality delivery within contracts. You’ll work with cross-functional teams to implement study strategies, manage risks, and drive financial performance.You will own relationships with key customers and guide the team to achieve milestones across multi-country studies. This role offers impact in shaping immuno-oncology and cell/gene therapy programs at IQVIA, with a hybrid work setup and strong emphasis on leadership and collaboration.
Compensaciones / Beneficios- Lead bid defense preparations and presentations with Business Development for large, multi-country studies
- Develop or support integrated study management plans with the core project team
- Oversee strategic delivery of clinical studies, optimizing speed, quality, and cost
- Serve as primary project liaison with customers and coordinate with IQVIA BD as needed
- Set objectives for the project team, monitor performance, and provide leadership feedback
- Collaborate with functional groups to achieve milestones and manage issues
- Monitor progress, communicate proactively to stakeholders, and manage risks and contingencies
- Coach and mentor junior team members to ensure global alignment and development
- Ensure study quality, manage quality risks, and implement CAPAs as needed
- Participate in executive committees as part of program leadership
- Ensure financial success through resource management, forecasting, and profitability
- Forecast opportunities, accelerate activities, and manage scope changes with customer agreement
- Capture lessons learned and promote continuous improvement
- Support corporate initiatives and act as a change advocate
- Provide input on team members’ performance and support staff development
- Bachelor’s degree in life sciences or related field with advanced knowledge of role
- 10+ years of clinical research experience, including 6+ years in project management
- Knowledge of clinical trials, regulatory requirements (ICH GCP, local laws) and protocol understanding
- Strong communication, presentation, negotiation, and customer management skills
- Problem solving, leadership, and organizational planning capabilities
- Ability to manage priorities, strategic thinking, and cross-functional collaboration
- Attention to quality, learning agility, and up-to-date knowledge
- Proficiency with MS Office (Word, Excel, PowerPoint) and IT literacy
- Experience in managing project finances, contracts, and change control
- Ability to work across geographies and understand cultural differences
- Hybrid work model
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